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Biology
(life cycles)
Alternation of generations in the life cycle of Rhabdias bufonis was discovered
by Mecznikow (1865) and first published by Leukart (1865). The comprehensive information
on the development of this species is expanded in the papers of Schaake (1931) and
Spieler and Schierenberg (1995). In this species, eggs of parasitic hermaphrodites
pass from the host lungs into the intestine, accumulate in colon and, thereafter,
are cast out of the host organism in faeces. The free-living stages develop in the
droppings. Larvae from the eggs of hermaphrodites reach maturity as males and females
of gonochoristic generation. The latter give rise to the hermaphroditic generation
larvae which develop in droppings up to the third stage. At this stage the larvae
become infective and are able to continue development only after the penetration into
the host.
Figure 1. Rhabdiasoid life cycle: strict alternation of two generations.
Railliet (1899) and Goodey (1924 a) failed to observe the gonochoristic generation
in R. fuscovenosa. This species was considered to develop directly, in contrast
to other species of the family. However, Chu (1936 b), after thorough examination
of the development of R. fuscovenosa in laboratory cultures and, with original
cultivation method applied, found out that the smaller part of hermaphroditic generation
progeny developed indirectly. The progeny of the latter underwent the metamorphosis
during the second moult and the third-stage larvae had filaroid morphology, in contrast
to rhabditoid homogonic infective larvae and infective larvae in other species. These
filariform larvae failed to infect the hosts. The author believed that both homogony
and heterogony were characteristic for the life cycles of all Rhabdiasidae (as they
were in Strongyloididae) but the former way predominated in amphibian parasites and
the latter one predominated in the species from reptiles. The hypothesis of Chu, however,
has not been confirmed by the other authors, who investigated the development of various
rhabdiasid species, even when Chu's method of cultivation has been applied (see, for
example, the works of Baker (1978) and Kuzmin (1997, 2000). Homogony was not found
in the life cycles of amphibian parasites, nor it was in the life cycles of species
from chameleons and lizards (i. e. R. gemellipara, R. chameleonis, Pneumonema
tiliquae, Entomelas spp.). The only two species that have been found to
possess the life cycles similar to that in R. fuscovenosa and Strongyloides
spp. were R. elaphe and R. agkistrodonis (Kuzmin 1999; Kuzmin and
Miskov 1999). Both species are the parasites of snakes. Heterogonic infective larvae
in these species are rhabditoid and morphologically similar to the homogonic ones.
Figure 2. Strongyloid life cycle, combination of heterogony and
homogony.
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